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Adding vitamin D3 to the dipeptidyl peptidase-4 inhibitor saxagliptin has the potential to protect β-cell function in LADA patients: A 1-year pilot study.

Authors :
Zhang, Ziwei
Yan, Xiang
Wu, Chao
Pei, Xieyi
Li, Xia
Wang, Xiangbing
Niu, Xiaohong
Jiang, Hongwei
Zeng, Xiaomin
Zhou, Zhiguang
Source :
Diabetes/Metabolism Research & Reviews; Jul2020, Vol. 36 Issue 5, p1-8, 8p
Publication Year :
2020

Abstract

<bold>Aims: </bold>This trial was conducted to explore the protective effect on β-cell function of adding vitamin D3 to DPP-4 inhibitors to treat patients with latent autoimmune diabetes in adults (LADA).<bold>Methods: </bold>60 LADA patients were randomized to group A (n = 21) - conventional therapy with metformin (1-1.7 g/day) and/or insulin treatment; group B (n = 20) - saxagliptin (5 mg/day) plus conventional therapy; and group C (n = 19) - vitamin D3 (2000 IU/day) plus saxagliptin and conventional therapy for 12 months. Fasting and 2-hour postprandial blood samples were collected to measure blood glucose, glycosylated hemoglobin and C-peptide levels at baseline and after 3, 6 and 12 months of treatment.<bold>Results: </bold>During the 12 months of follow-up, the levels of fasting C-peptide (FCP), 2-hour postprandial C-peptide (PCP) and the C-peptide index (CPI, serum C-peptide-to-plasma glucose level ratio) were maintained in group C. In contrast to those in group A and group B, FCP levels decreased significantly in group B, and CPI levels declined significantly in group A during the 1-year treatment (P < .05). Additionally, the levels of GADA titers in group C significantly decreased compared with those at baseline (P < .05), but no significant differences in GADA titers levels were detected in group A and group B. No significant differences were found among the three groups in the levels of FCP, PCP, the CPI or GADA titers.<bold>Conclusions: </bold>The data suggested that adding 2000 IU/day vitamin D3 to saxagliptin might preserve β-cell function in patients with LADA. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
15207552
Volume :
36
Issue :
5
Database :
Complementary Index
Journal :
Diabetes/Metabolism Research & Reviews
Publication Type :
Academic Journal
Accession number :
144405981
Full Text :
https://doi.org/10.1002/dmrr.3298